![Loading...](https://link.springer.com/static/c4a417b97a76cc2980e3c25e2271af3129e08bbe/images/pdf-preview/spacer.gif)
-
Article
Open AccessGene expression analysis in Fmr1KO mice identifies an immunological signature in brain tissue and mGluR5-related signaling in primary neuronal cultures
Fragile X syndrome (FXS) is a neurodevelopmental disorder whose biochemical manifestations involve dysregulation of mGluR5-dependent pathways, which are widely modeled using cultured neurons. In vitro phenotyp...
-
Chapter
Information Processing at the Genomics Level
A central objective in biology is to identify and characterize the mechanistic underpinnings (e.g., gene, protein interactions) of a biological phenomenon (e.g., a phenotype). Today, it is technologically feas...
-
Article
Gene expression profiling of Duchenne muscular dystrophy skeletal muscle
The primary cause of Duchenne muscular dystrophy (DMD) is a mutation in the dystrophin gene, leading to absence of the corresponding protein, disruption of the dystrophin-associated protein complex, and substa...